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Job Title: Part-Time Clinical Research Endocrinologist
Location: Scottsdale, AZ
Schedule: Part-Time (0-8 hours/week)
Start Date: Within 0-6 months

About the Role
We are seeking a board-certified Endocrinologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in Phase I-IV clinical trials. The physician will provide clinical oversight, ensure protocol compliance, monitor patient safety, and collaborate with research staff and sponsors to support high-quality trial execution.

Key Responsibilities

Serve as PI or Sub-I across endocrinology and multi-therapeutic studies
Conduct medical screenings, assessments, and physical exams
Ensure patient safety and compliance with study protocols, ICH-GCP, and regulatory standards
Review and document subject data, adverse events, and study outcomes
Collaborate with coordinators, nurses, CROs, and sponsors
Participate in site visits, audits, and investigator meetings

Qualifications

MD or DO with an active Arizona medical license
Board-certified in Endocrinology
DEA license and BLS/ACLS certification
Prior clinical research experience preferred (training available)
Strong communication and organizational skills

Benefits

Flexible part-time schedule
Opportunity to contribute to advancing endocrinology treatments
Professional growth in clinical research

If you're interested, please let me know a convenient time to chat, or feel free to contact me directly at or via email at .

","shortDescription","

Job Title: Part-Time Clinical Research Endocrinologist
Location: Scottsdale, AZ
Schedule:Under general supervision of the Clinical Trials Office (CTO), Manager of Clinical Operations coordinates complex data management activities involving NCI Cooperative group, Investigator Initiated and industry-sponsored oncology trials at the Medical University of South Carolina (MUSC). Provides core support for protocol management, patient and data management for oncology research studies conducted at the Hollings Cancer Center. Professional judgment is required regarding patient management and research protocol compliance.

Responsibilities

35% – Timely and accurately submits data to established research bases including the National Cancer Institute, industry sponsors and MUSC. Maintains subject research charts and submits data for assigned patient caseload. Patient management will include multiple disease programs and protocols. Protocol management will include NCI cooperative groups, investigator initiated and industry sponsored oncology trials at the MUSC. Interprets protocols, informed consents and case report forms in order to develop and use study related forms, data, calendars and documents according to accepted clinical trials professional standards. Meticulous data management is required for assigned studies and patient caseload. Chart extraction, retrieval of outside medical records, admission records, clinic visits, and all source is required. Maintenance of research subject records and case report forms is essential. Case report submission may include patient reported outcome questionnaires, radiologic scans, reports and staging tests. Proactively plan, prioritize and manage responsibilities to ensure timely and accurate data submission to specified research bases. Data submission is timely and accurate per the protocol, study participant calendar, and source documents. Ensures data is submitted according to sponsor mandated time frames and in a manner that affords maximum accuracy. Data submission will include query resolution, and adverse event and concomitant medication logs. Maintains established workflows to identify data needs of numerous trials within multiple disease groups and communicates data entry needs to study team.

25% – Timely and accurately coordinates the process to request, prepare, ship and/or submit requirements per protocol and applicable study manuals. Submissions may include but are not limited to radiology images, EKGs, pathology specimens, blood borne pathogens and other biologic specimens. Prepares, transports, and handles blood borne pathogens and other biologic specimens in accordance with OSHA and IATA guidelines. Responsible for laboratory supply kit management including storage, inventory, and ordering to maintain lab kit supply. Lab kit management will require utilization of sponsor specific vendors along with internal lab kit and specimen management tracking systems and processes. Responsible for preparing kits for each study participant and ensuring collection and shipment per Federal guidelines. Prepares and ships frozen and ambient specimens, including central labs, pharmacokinetic and pharmacodynamics. Preparation includes professional communication and collaboration with colleagues, CTO Data Core, Nexus SCTR services, translational, fast flow and phlebotomy labs to facilitate protocol compliance. Completes required specimen submission case report forms, protocol specific shipping procedures and enters specimen tracking data on designated NCI and or sponsor vendor website including CTSU OPEN funding. Responsible for maintaining sponsor imaging portal access and transmitting radiology images per the protocol and sponsor requirements. Responsible for addressing queries issued by the sponsor and/or imaging vendor, including effective communication with the study team and MUSC radiology department as needed to resolve queries.

15% – Coordinates trial follow up patient visits and related activities to accurately meet protocol requirements. Provides protocol specific information for study coordinators, physicians, nurses, and study participants. Coordinates required follow-up requirements with patient, medical staff, nursing staff and ancillary hospital personnel. Ensures that follow-up assessments are completed per protocol to meet study requirements. Works closely with clinical nurse staff to coordinate patient care to meet protocol standards. Consults with the investigator to assess study participant for response to protocol therapy including toxicity assessment and disease status. Ensures timely clinical trial management system (CTMS) database updates to reflect accurate patient status within 24 hours. Links patient research visits in Epic prior to scheduled study visit date. Ensures source documentation is located within patient research chart for source documentation verification per departmental SOPs.

15% – Timely and accurately submits Adverse Events, Serious Adverse Events, and other reportable events to the NCI, sponsors, IRB and DSMC per federal guidelines and institutional policies. Proactively plans to ensure comprehensive reports are submitted per the Clinical Trials Office standard operating procedures, to ensure submission to the IRB of record and study sponsor is completed within the permitted timeframe. Reportable events requiring expedited submission may include adverse events, serious adverse events, correspondence from the sponsor, protocol deviations, or any other documents requiring review and submission to the IRB. Protocol deviations will be reported to the clinical trials office regulatory unit per departmental processes. Prepares and submits initial and follow up adverse events as required and until resolution of adverse events. Responsible for contemporaneous completion of adverse event logs. Coordinates the reporting of adverse events and serious adverse events based on the NCI Common Terminology Criteria for Adverse Events (CTCAE) and protocol requirements. Adverse Event tracking is completed and maintained for numerous research subjects on various studies. Participates in staff training on NCI CTC adverse event reporting. This training may include Adverse Events, Serious Adverse Events, baseline medical history, and Adverse Event and concomitant medication tracking logs. Items that are outstanding per sponsor monitoring visit letters will be addressed and closed within 4 weeks of receiving the monitoring letter, or by the date of the monitor’s next site visit, whichever is earlier.

10% – Attends and actively participates in staff training and education regarding data management and clinical operations processes. Trainings include but are not limited to CTO staff meetings, Clinical Operations Update Meetings, huddles and team meetings. Works effectively and cooperatively with colleagues to assist routine monitor visits. Utilizes office tools including sharepoint, clinical trial management system, Clinical Data Center (CDC), and other applicable platforms. Collaborates with Study Coordinators as needed with participant protocol visits including participant questionnaires, escorting study participants to various locations on campus, picking up IDS oral study medication, and transporting study supplies. Completes other research tasks and projects as assigned. Assists with the development of educational materials specific to each study and disseminates to appropriate staff. Staff training may include CTSU, NCI data bases, CTMS, SharePoint, EPIC EMR, EPIC patient linking of research participants, collection and shipping of specimens, requesting internal and external radiologic images and submitting to study sponsor.

Minimum Requirements
A bachelor's degree and two years of relevant program experience.

Physical Requirements

Ability to perform job functions in an upright position. (Frequent)

Ability to perform job functions in a seated position. (Frequent)

Ability to perform job functions while walking/mobile. (Frequent)

Ability to work indoors. (Continuous)

Ability to work outdoors in all weather and temperature extremes. (Infrequent)

Ability to work in confined/cramped spaces. (Infrequent)

Ability to perform job functions from kneeling positions. (Infrequent)

Ability to squat and perform job functions. (Infrequent)

Ability to perform 'pinching' operations. (Infrequent)

Ability to fully use both hands/arms. (Frequent)

Ability to perform repetitive motions with hands/wrists/elbows and shoulders. (Frequent)Ability to reach in all directions. (Frequent)

Possess good finger dexterity. (Continuous)

Ability to maintain tactile sensory functions. (Continuous)

Ability to lift and carry 15 lbs., unassisted. (Infrequent)

Ability to lower objects, up to 15 lbs., from height of 36 inches to floor level, unassisted. (Infrequent)

Ability to push/pull objects, up to 15 lbs., unassisted. (Infrequent)

Ability to maintain 20/40 vision, corrected, in one eye or with both eyes. (Continuous)

Ability to see and recognize objects close at hand. (Continuous)

Ability to see and recognize objects at a distance. (Frequent)

Ability to determine distance/relationship between objects; depth perception. (Frequent)

Good peripheral vision capabilities. (Continuous)

Ability to maintain hearing acuity, with correction. (Continuous)

Ability to perform gross motor functions with frequent fine motor movements. (Frequent)

Equal Opportunity Statement
The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and/or federal regulations. All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need. Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees.

#J-18808-Ljbffr
","Job Overview
Under general supervision of the Clinical Trials Office (CTO), Manager of Clinical Operations coordinates complex data management ...","UNIV-Research Data Coordinator-Hollings Cancer Center",[89],["B","3522859413"],"Work at MUSC Health","1 days ago","/jobs/3522859413-univ-research-data-coordinator-hollings-cancer-center","Charleston, SC, United States","/jobs?keyword=MUSC+Health","/jobs?location=Charleston%2C+SC%2C+United+States","/jobs?keyword=UNIV-Research+Data+Coordinator-Hollings+Cancer+Center",{"_65":66,"_67":90,"_69":91,"_71":92,"_73":93},"Charleston","Charleston, SC, United States, 29408","SC","29408",["D",1776863060707],"Medix","Title: Senior Medical Director / Principal Investigator Clinical Research
Location: On-site, Austin, Texas 78738
Employment Type: Full-time, W-2
Hours: Monday - Friday, 8 AM - 5 PM

About the Role

Medix is seeking an experienced Senior Medical Director (SMD) to lead clinical research programs and provide strategic medical leadership across multiple therapeutic areas. This role is ideal for a research-driven physician passionate about advancing clinical innovation and improving patient outcomes through evidence-based medicine.

As the Senior Medical Director, you ll serve as a Principal or Sub-Investigator, oversee study execution, ensure regulatory compliance, and mentor junior investigators. You ll also collaborate with sponsors, CROs, and community partners to drive clinical trial success and organizational growth.

Key Responsibilities

Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials conducted at our Clinical Research Center.
Ensure participant safety and data integrity in compliance with GCP/HSP guidelines.
Collaborate with leadership to identify new research programs and therapeutic areas.
Build and maintain partnerships with community physicians and organizations to support patient recruitment and enrollment.
Review protocols, assess study feasibility, and provide clinical oversight during execution.
Mentor and train clinical staff and investigators on study protocols and therapeutic areas.
Participate in strategic discussions shaping the research center s future direction.
Maintain clinical expertise in adult chronic disease management.

Qualifications

MD or DO degree from an accredited U.S. medical school.
Active medical license and board certification required.
Minimum 8 years of experience in U.S. community healthcare, including chronic disease management.
At least 2 years of experience in FDA clinical research as a Principal or Sub-Investigator.
Experience as a PI on GLP-1 studies lasting 12 months or longer preferred but not required
Strong leadership, communication, and analytical skills.

Apply today to learn more about this Senior Medical Director role or explore other opportunities in clinical research with Medix!

","Title: Senior Medical Director / Principal Investigator Clinical Research
Location: On-site, Austin, Texas 787...","Internal Medicine Physician",[107],["B","3522404961"],"Work at Medix","/jobs/3522404961-internal-medicine-physician","Austin, TX, United States","/jobs?keyword=Medix","/jobs?location=Austin%2C+TX%2C+United+States","/jobs?keyword=Internal+Medicine+Physician",{"_65":66,"_67":108,"_69":109,"_71":110,"_73":111},"Austin","Austin, TX, United States, 78738","TX","78738",["D",1776863013151],"Clinical Trial Physician (Endocrinologist) - 8 hours per week
Location: Huntington Beach, CA
Schedule: Flexible Part-Time (0-8 hours per week)
Start Date: Within 0-6 months Position Summary
We are seeking a board-certified Endocrinologist to serve as Principal Investigator or Sub-Investigator in our current and upcoming clinical trials. The Endocrinologist will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research staff to maintain high-quality trial execution.
Key Responsibilities
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) in clinical trials.
Conduct medical evaluations and assess participant eligibility.
Monitor patient safety, adverse events, and treatment outcomes.
Review and sign study-related documentation according to protocol and regulations.
Collaborate with study coordinators, nurses, and research staff.
Attend protocol training and maintain adherence to Good Clinical Practice (GCP).
Qualifications
MD or DO with an active medical license in California.
Board-certified Endocrinologist.
Interest in clinical research (prior experience preferred; training provided if needed).
Strong communication and organizational skills.
Compensation & Benefits
$100-$200 per hour, based on study complexity.
Flexible schedule (0-8 hours/week).
Professional growth in clinical research.
Opportunity to contribute to advancing endocrinology treatments.
","Clinical Trial Physician (Endocrinologist) - 8 hours per week
Location: Huntington Beach, CA
Sch...",[120],["B","3522516731"],"/jobs/3522516731-endocrinology-physician","Huntington Beach, CA, United States","/jobs?location=Huntington+Beach%2C+CA%2C+United+States",{"_65":66,"_67":121,"_69":122,"_71":123,"_73":124},"Huntington Beach","Huntington Beach, CA, United States, 92605","CA","92605",["D",1776863013170],"
Job Title: Clinical Research Rheumatologist
Location: Scottsdale, AZ
Schedule: Part-Time (0-8 hours/week)
Start Date: Within 0-6 months
About the Role
We are seeking a board-certified Rheumatologist to serve as a Principal Investigator (PI) or Sub-Investigator (Sub-I) in Phase I-IV clinical trials. The physician will oversee study participants, ensure protocol compliance, monitor patient safety, and collaborate with research staff and sponsors to deliver high-quality clinical research.
Key Responsibilities
Serve as PI or Sub-I in rheumatology and multi-therapeutic clinical trials
Conduct medical screenings, assessments, and physical exams
Provide clinical oversight and ensure adherence to protocols, ICH-GCP, and regulatory standards
Document subject data, adverse events, and study outcomes accurately
Collaborate with study coordinators, nurses, CROs, and sponsors
Participate in site visits, audits, and investigator meetings
Qualifications
MD or DO with an active Arizona medical license
Board-certified in Rheumatology
DEA license and BLS/ACLS certification
Clinical research experience preferred (training available)
Strong communication and organizational skills
Benefits
Flexible part-time schedule
Opportunity to contribute to advancing rheumatology treatments
Professional growth in clinical research

If you're interested, please let me know a convenient time to chat, or feel free to contact me directly at or via email at .
","
Job Title: Clinical Research Rheumatologist
Location: Scottsdale, AZ
Schedule: Part-Tim...","Rheumatology Physician",[133],["B","3522516704"],"/jobs/3522516704-rheumatology-physician","/jobs?keyword=Rheumatology+Physician",{"_65":66,"_67":68,"_69":70,"_71":72,"_73":74},1072,"name","Hearst Television","agency","logo","slug","hearst-television","
Every career with Hearst Television is like a story. How it develops, where it takes you, the milestones you reach along the way – you’ve got a lot to look forward to as your unique career story unfolds. Hearst Television, a subsidiary of Hearst, owns and operates local television and radio stations serving nearly three dozen U.S. cities, reaching 24 million U.S. television households. Through its partnership with nearly all major networks, Hearst Television distributes national content across more than 120 video channels, including programming from ABC, NBC, CBS, CW, MY Net, MeTV, This TV, Estrella, and more. Hearst Television is recognized as one of the industry's premier companies. It has been honored with numerous awards for distinguished journalism and industry innovation, including the Walter Cronkite Award for political journalism, the national Edward R. Murrow Award, the DuPont-Columbia Award, and the George Foster Peabody Award.
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As a Principal Investigator, you will provide medical oversight and leadership for oncology clinical trials. You will be responsible for ensuring subject safety, regulatory compliance, and protocol adherence throughout the duration of the study. Our site team will support you with daily operations, allowing you to focus on medical decision-making and oversight.

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As a Principal Investigator, you will provide medical oversight and leadership for oncology clinical trials. You will be responsible for ensurin...",[192],"salaryMin","salaryMax","salaryDescription","url","https://job-api.jobget.com/v1/job/97980533623?context=WyIzQ0pmUGo0VXhvNFhBaFM1MVBSbHU0UGg2K2RrajdPYjhUcU1JK0pDQnVVWDlTck5LeCtKMXEwOEc1Zy80K0g1ZlRyQWRoTG5Tb2RHVEt2cnY0YjkvZDU0QjA4eUpiWVdBejdHcTBtYVRaQXhyTTJGIiwicHU3bEJyUFRETVVFbllELyIsIkJQSEMwdTNjREFQMjlaL2VrTVpQREE9PSJd&jg_eid=eba098d2-dd35-499b-a3c7-562098453c9d","companyDescription","companyWebsite","isManualPosted","costPerClick",0.24,"/jobs/3522742264-oncology-medical-oncology-physician","fullUrl","https://www.mediabistro.com/jobs/3522742264-oncology-medical-oncology-physician","strippedDescription","As a Principal Investigator, you will provide medical oversight and leadership for oncology clinical trials. 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